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EP0605090B1 - Curing silica precursors by exposure to nitrous oxide - Google Patents

Curing silica precursors by exposure to nitrous oxide Download PDF

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Publication number
EP0605090B1
EP0605090B1 EP93308383A EP93308383A EP0605090B1 EP 0605090 B1 EP0605090 B1 EP 0605090B1 EP 93308383 A EP93308383 A EP 93308383A EP 93308383 A EP93308383 A EP 93308383A EP 0605090 B1 EP0605090 B1 EP 0605090B1
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EP
European Patent Office
Prior art keywords
coating
silica
substrate
silica precursor
nitrous oxide
Prior art date
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Application number
EP93308383A
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German (de)
French (fr)
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EP0605090A1 (en
Inventor
David Stephen Ballance
Loren Andrew Haluska
Mark Jon Loboda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Silicones Corp
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Dow Corning Corp
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104—Forming layers
    • H01L21/02107—Forming insulating materials on a substrate
    • H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
    • H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
    • H01L21/02282—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process liquid deposition, e.g. spin-coating, sol-gel techniques, spray coating
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    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • C—CHEMISTRY; METALLURGY
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    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
    • C04B41/49—Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Organo-clay compounds; Organo-silicates, i.e. ortho- or polysilicic acid esters ; Organo-phosphorus compounds; Organo-inorganic complexes
    • C04B41/4905—Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Organo-clay compounds; Organo-silicates, i.e. ortho- or polysilicic acid esters ; Organo-phosphorus compounds; Organo-inorganic complexes containing silicon
    • C04B41/4922—Compounds having one or more carbon-to-metal or carbon-to-silicon linkages ; Organo-clay compounds; Organo-silicates, i.e. ortho- or polysilicic acid esters ; Organo-phosphorus compounds; Organo-inorganic complexes containing silicon applied to the substrate as monomers, i.e. as organosilanes RnSiX4-n, e.g. alkyltrialkoxysilane, dialkyldialkoxysilane
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
    • C04B41/81—Coating or impregnation
    • C04B41/82—Coating or impregnation with organic materials
    • C04B41/84—Compounds having one or more carbon-to-metal of carbon-to-silicon linkages
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104—Forming layers
    • H01L21/02107—Forming insulating materials on a substrate
    • H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
    • H01L21/02205—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition
    • H01L21/02208—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si
    • H01L21/02214—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si the compound comprising silicon and oxygen
    • H01L21/02216—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates the layer being characterised by the precursor material for deposition the precursor containing a compound comprising Si the compound comprising silicon and oxygen the compound being a molecule comprising at least one silicon-oxygen bond and the compound having hydrogen or an organic group attached to the silicon or oxygen, e.g. a siloxane
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
    • H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
    • H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
    • H01L21/314—Inorganic layers
    • H01L21/316—Inorganic layers composed of oxides or glassy oxides or oxide based glass
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
    • H01L21/48—Manufacture or treatment of parts, e.g. containers, prior to assembly of the devices, using processes not provided for in a single one of the subgroups H01L21/06 - H01L21/326
    • H01L21/4803—Insulating or insulated parts, e.g. mountings, containers, diamond heatsinks
    • H01L21/481—Insulating layers on insulating parts, with or without metallisation
    • H—ELECTRICITY
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    • H01L23/00—Details of semiconductor or other solid state devices
    • H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
    • H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
    • H01L23/291—Oxides or nitrides or carbides, e.g. ceramics, glass
    • H—ELECTRICITY
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    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00—Details of semiconductor or other solid state devices
    • H01L23/48—Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor
    • H01L23/488—Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor consisting of soldered or bonded constructions
    • H01L23/498—Leads, i.e. metallisations or lead-frames on insulating substrates, e.g. chip carriers
    • H01L23/49866—Leads, i.e. metallisations or lead-frames on insulating substrates, e.g. chip carriers characterised by the materials
    • H01L23/49894—Materials of the insulating layers or coatings
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00844—Uses not provided for elsewhere in C04B2111/00 for electronic applications
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104—Forming layers
    • H01L21/02107—Forming insulating materials on a substrate
    • H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
    • H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
    • H01L21/02123—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon
    • H01L21/02126—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer the material containing silicon the material containing Si, O, and at least one of H, N, C, F, or other non-metal elements, e.g. SiOC, SiOC:H or SiONC
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001—Technical content checked by a classifier
    • H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Definitions

  • the present invention relates to a method of forming silica-containing ceramic coatings on substrates such as electronic devices. These coatings can be used to provide hermetic protection to the underlying substrate or they can be used as dielectric layers.
  • the present invention also uses nitrous oxide to convert various silica precursors to silica-containing coatings at low temperatures.
  • the present invention is directed to a method of forming a silica-containing ceramic coating on a substrate.
  • the method comprises first applying a silica precursor coating comprising hydrolyzed or partially hydrolyzed R n Si(OR) 4-n on the substrate, in which each R is independently an aliphatic, alicyclic or aromatic substituent of 1-20 carbon atoms and n is 0-3.
  • R is independently an aliphatic, alicyclic or aromatic substituent of 1-20 carbon atoms and n is 0-3.
  • the coated substrate is then heated in an atmosphere containing nitrous oxide at a temperature sufficient to convert the coating to a silica-containing ceramic coating. This method is especially valuable for forming coatings on electronic devices.
  • the present invention adopts the use of nitrous oxide (N 2 O) to accelerate the conversion of silica precursors to silica-containing coatings at low temperatures.
  • This invention has an impact on the use of silica precursors for coating temperature sensitive substrates such as electronic devices since it avoids various problems with prior art conversion processes and agents. Such problems have included explosion and environmental concerns, the use of elevated temperatures, corrosivity of the curing agents, cracking and modification of the coating and availability of materials.
  • coatings on substrates such as electronic devices or electronic circuits which are temperature sensitive and which require high quality coatings.
  • Such coatings could serve, for example, as protective or dielectric coatings, interlevel dielectric layers, doped dielectric layers to produce transistor like devices, pigment loaded binder systems containing silicon to produce capacitor and capacitor like devices, multilayer devices, 3-D devices, silicon on insulator devices, coatings for superconductors, super lattice devices and the like.
  • the choice of substrates to be coated by the instant invention is limited only by the need for thermal and chemical stability of the substrate under the conditions used.
  • non-electronic substrates such as plastics including, for example, polyimides, epoxides, polytetrafluoroethylene and copolymers thereof, polycarbonates, acrylics, polyesters and the like.
  • silica-containing ceramic is meant to include both amorphous silica (SiO 2 ) materials as well as amorphous silica-like materials that are not fully free of residual carbon, silanol (Si-OH) and/or hydrogen and which may contain additional ceramic materials. Such silica-containing ceramic materials may have variable densities depending on the temperature and time of heating.
  • electroactive device or “electronic circuit” include, but are not limited to, silicon based devices, gallium arsenide based devices, focal plane arrays, opto-electronic devices, photovoltaic cells and optical devices.
  • a silica-containing ceramic coating is formed on a substrate by a process which comprises coating the substrate with a silica precursor composition comprising hydrolyzed or partially hydrolyzed R n Si(OR) 4-n and then heating the coated substrate in an environment comprising nitrous oxide.
  • the silica precursor material useful herein includes hydrolyzed or partially hydrolyzed compounds of the formula R n Si(OR) 4-n , in which each R is independently an aliphatic, alicyclic or aromatic substituent of 1-20 carbon atoms, preferably 1-4, such as an alkyl (e.g., methyl, ethyl, propyl), alkenyl (e.g., vinyl or allyl), alkynyl (e.g., ethynyl), cyclopentyl, cyclohexyl and phenyl.
  • alkyl e.g., methyl, ethyl, propyl
  • alkenyl e.g., vinyl or allyl
  • alkynyl e.g., ethynyl
  • cyclopentyl cyclohexyl and phenyl.
  • n is 0-3, preferably 0 or 1.
  • Specific compounds of this type include, for example, methyltriethoxysilane, phenyltriethoxysilane, diethyldiethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, vinyltrimethoxysilane, tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane and tetrabutoxysilane.
  • the silicon atoms therein may be bonded to C, OH or OR groups, but a substantial portion of the material is believed to be condensed in the form of soluble Si-O-Si resins.
  • the precursor most preferably comprises compounds in which each R is independently an diphatic substituent of 1-4 carbon atoms, and n is 0 or 1.
  • Compounds in which n 2 or 3 are generally not used alone as volatile cyclic structures are generated during pyrolysis, but small amounts of said compounds may be cohydrolyzed with other silanes to prepare useful preceramic materials.
  • the above silica precursor coating material may also contain other ceramic oxide precursors.
  • ceramic oxide precursors include compounds of various metals such as aluminum, titanium, zirconium, tantalum, niobium and/or vanadium as well as various non-metallic compounds such as those of boron or phosphorous which may be dissolved in solution, hydrolyzed and subsequently pyrolyzed, at relatively low temperatures and relatively rapid reaction rates to form ceramic oxide coatings.
  • the above ceramic oxide precursor compounds generally have one or more hydrolyzable groups bonded to the above metal or non-metal, depending on the valence of the metal.
  • the number of hydrolyzable groups to be included in these compounds is not critical as long as the compound is soluble in the solvent. Likewise, selection of the exact hydrolyzable substituent is not critical since the substituents are either hydrolyzed or pyrolyzed out of the system.
  • Typical hydrolyzable groups include alkoxy, such as methoxy, propoxy, butoxy and hexoxy, acyloxy, such as acetoxy or other organic groups bonded to said metal or nonmetal through an oxygen such as acetylacetonate.
  • Specific compounds, therefore, include zirconium tetracetylacetonate, titanium dibutoxy diacetylacetonate, aluminum triacetylacetonate and tetraisobutoxy titanium.
  • the silica precursor When the silica precursor is to be combined with one of the above ceramic oxide precursors, generally it is used in an amount such that the final ceramic coating contains 70 to 99.9 percent by weight SiO 2 .
  • the above silica precursor and, optionally, any ceramic oxide precursors are applied to the surface of a substrate.
  • a preferred method involves dissolving the silica precursor in a solvent to form a solution or dispersion which is applied to the surface of the substrate.
  • Various facilitating measures such as stirring and/or heating may be used to dissolve or disperse the silica precursor and create a more uniform application solution.
  • Solvents which may be used include any agent or mixture of agents which will dissolve or disperse the silica precursor to form a homogenous solution without affecting the resultant coating.
  • solvents can include, for example, alcohols such as ethyl or isopropyl, aromatic hydrocarbons such as benzene or toluene, alkanes such as n-heptane or dodecane, ketones, esters, glycol ethers or cyclic dimethylpolysiloxanes, in an amount sufficient to dissolve the above materials to low solids. Generally, enough of the above solvent is used to form a 0.1-50 weight percent solution.
  • the solution comprising the silica precursor, solvent and, optionally, a modifying ceramic oxide precursor is then coated onto the substrate.
  • the method of coating can be spin coating, dip coating, spray coating or flow coating. Other equivalent means, however, are also deemed to be within the scope of this invention.
  • the solvent is then allowed to evaporate from the coated substrate resulting in the deposition of a silica precursor coating.
  • Any suitable means of evaporation may be used such as simple air drying by exposure to an ambient environment, by the application of a vacuum or mild heat (eg., less than 50°C) or during the early stages of the heat treatment. It is to be noted that when spin coating is used, the additional drying period is minimized as the spinning process drives off the solvent.
  • the silica precursor coating is applied, it is then heated in an environment containing nitrous oxide at a temperature sufficient to convert it to a silica-containing material. During this conversion, factors such as nitrous oxide gas concentration, gas exposure time, temperature and heating time all need to be controlled.
  • nitrous oxide used in this process is known in the art and commercially available. It may be used in this invention in its neat form or it may be diluted in additional gases (eg., inert gases such as argon or nitrogen or reactive gases such as air, ammonia or amines) to a concentration sufficient to convert the silica precursor to silica at a desirable rate under the temperature conditions chosen.
  • additional gases eg., inert gases such as argon or nitrogen or reactive gases such as air, ammonia or amines
  • the silica precursor coating is generally exposed to this gas for a time sufficient to convert the silica precursor to silica. Generally, times in the range of several minutes to several hours are useful (eg., 2 minutes to 2 hours). This exposure can occur during the ramp-up, during the heat soak or during ramp-down.
  • the silica precursor may be concomitantly or sequentially exposed to other reactive gases which assist in conversion.
  • other reactive gases e.g., water
  • the temperatures useful herein are in the range of 100°C. to 600°C. Higher and lower temperatures, however, are also contemplated in the invention. For example, lower temperatures may be used but they often result in incomplete conversion of the silica precursor and insufficient densification of the ceramic. Similarly, higher temperatures (eg., 1000°C.) may be used but the need for nitrous oxide is diminished since the silica precursors can generally be converted to silica at such temperatures in air.
  • the coated substrates are heated under the nitrous oxide containing environment for a time sufficient to convert the silica precursor to silica. Time periods in the range of a few minutes for very thin films to several hours for very thick films, depending on the temperature, are generally useful herein. It is particularly preferred to heat the coated substrates at a temperature of 200-500°C. for 1-3 hours.
  • any method of heating such as the use of a quartz tube furnace, a convection oven, reverse direction processing as described in US Patent Application 07/633,707, now allowed, and assigned to the same assignee hereof or radiant or microwave energy is generally functional herein.
  • the rate of heating is generally not a critical factor, but it is most practical and preferred to heat the substrate as rapidly as possible.
  • a thin (less than 2 micrometers) silica-containing ceramic planarizing coating is produced on the substrate.
  • the coating smooths the irregular surfaces of various substrates and has excellent adhesive properties.
  • the coating may be covered by other coatings such as additional SiO 2 layers, silicon containing coatings, silicon carbon containing coatings, silicon nitrogen containing coatings, silicon oxygen nitrogen containing coatings and/or silicon nitrogen carbon containing coatings.
  • additional SiO 2 layers silicon containing coatings, silicon carbon containing coatings, silicon nitrogen containing coatings, silicon oxygen nitrogen containing coatings and/or silicon nitrogen carbon containing coatings.
  • Coatings produced by the instant invention possess low defect density and are useful on electronic devices as protective coatings, as corrosion resistant and abrasion resistant coatings, as temperature and moisture resistant coatings, as dielectric layers and as a diffusion barrier against ionic impurities such as sodium and chloride.
  • a 2.5 cm (1 inch) square silicon wafer was spin coated with a 10 wt. % solution of partially hydrolyzed ethylorthosilicate in isopropyl alcohol and n-Butanol solvents at a spin speed of 3000 RPM for 20 seconds.
  • the coated wafer was heated to 350°C. for 3 hours in an environment comprising 100% nitrous oxide.
  • FTIR analysis after the heat treatment showed only a trace of SiOH remained.
  • the coating thickness was 289 nm (2888 angstroms) and the refractive index was 1.452 at 405 nm.
  • a 2.5 cm (1 inch) square silicon wafer was spin coated with a 10 wt. % solution of partially hydrolyzed ethylorthosilicate in isopropyl alcohol and n-butanol solvents at a spin speed of 3000 RPM for 20 seconds.
  • the coated wafer was heated to 425°C. for 3 hours in an environment comprising 100% nitrous oxide.
  • FTIR analysis after the heat treatment showed essentially all of the SiOH was removed.
  • the coating thickness was 286 nm (2863 angstroms) and the refractive index was 1.456 at 405 nm.

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  • Chemical & Material Sciences (AREA)
  • Ceramic Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Computer Hardware Design (AREA)
  • Microelectronics & Electronic Packaging (AREA)
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  • Silicon Compounds (AREA)
  • Formation Of Insulating Films (AREA)
  • Laminated Bodies (AREA)

Description

  • The present invention relates to a method of forming silica-containing ceramic coatings on substrates such as electronic devices. These coatings can be used to provide hermetic protection to the underlying substrate or they can be used as dielectric layers. The present invention also uses nitrous oxide to convert various silica precursors to silica-containing coatings at low temperatures.
  • The use of silica coatings derived from resinous precursors on substrates such as electronic devices is known from U.S. Patent No. 4,749,631; U.S. Patent No. 4,842,888; U.S. Patent 5,116,637; U.S. Patent No. 4,239,811 and EP Patent Application 93 305 375 filed 7/8/93 and assigned to the same assignee hereof.
  • The present invention is directed to a method of forming a silica-containing ceramic coating on a substrate. The method comprises first applying a silica precursor coating comprising hydrolyzed or partially hydrolyzed RnSi(OR)4-n on the substrate, in which each R is independently an aliphatic, alicyclic or aromatic substituent of 1-20 carbon atoms and n is 0-3. The coated substrate is then heated in an atmosphere containing nitrous oxide at a temperature sufficient to convert the coating to a silica-containing ceramic coating. This method is especially valuable for forming coatings on electronic devices.
  • The present invention adopts the use of nitrous oxide (N2O) to accelerate the conversion of silica precursors to silica-containing coatings at low temperatures. This invention has an impact on the use of silica precursors for coating temperature sensitive substrates such as electronic devices since it avoids various problems with prior art conversion processes and agents. Such problems have included explosion and environmental concerns, the use of elevated temperatures, corrosivity of the curing agents, cracking and modification of the coating and availability of materials.
  • Since the process of the present invention solves these problems, it is particularly valuable for the deposition of coatings on substrates such as electronic devices or electronic circuits which are temperature sensitive and which require high quality coatings. Such coatings could serve, for example, as protective or dielectric coatings, interlevel dielectric layers, doped dielectric layers to produce transistor like devices, pigment loaded binder systems containing silicon to produce capacitor and capacitor like devices, multilayer devices, 3-D devices, silicon on insulator devices, coatings for superconductors, super lattice devices and the like. The choice of substrates to be coated by the instant invention, however, is limited only by the need for thermal and chemical stability of the substrate under the conditions used. It is also contemplated, therefore, that the process of the invention could be used on non-electronic substrates such as plastics including, for example, polyimides, epoxides, polytetrafluoroethylene and copolymers thereof, polycarbonates, acrylics, polyesters and the like.
  • As used in the present invention, the expression "silica-containing ceramic" is meant to include both amorphous silica (SiO2) materials as well as amorphous silica-like materials that are not fully free of residual carbon, silanol (Si-OH) and/or hydrogen and which may contain additional ceramic materials. Such silica-containing ceramic materials may have variable densities depending on the temperature and time of heating. The expressions "electronic device" or "electronic circuit" include, but are not limited to, silicon based devices, gallium arsenide based devices, focal plane arrays, opto-electronic devices, photovoltaic cells and optical devices.
  • In the present invention, a silica-containing ceramic coating is formed on a substrate by a process which comprises coating the substrate with a silica precursor composition comprising hydrolyzed or partially hydrolyzed RnSi(OR)4-n and then heating the coated substrate in an environment comprising nitrous oxide.
  • The silica precursor material useful herein includes hydrolyzed or partially hydrolyzed compounds of the formula RnSi(OR)4-n, in which each R is independently an aliphatic, alicyclic or aromatic substituent of 1-20 carbon atoms, preferably 1-4, such as an alkyl (e.g., methyl, ethyl, propyl), alkenyl (e.g., vinyl or allyl), alkynyl (e.g., ethynyl), cyclopentyl, cyclohexyl and phenyl. The value of n is 0-3, preferably 0 or 1. Some of these materials are commercially available, for example, under the tradename ACCUGLASS. Specific compounds of this type include, for example, methyltriethoxysilane, phenyltriethoxysilane, diethyldiethoxysilane, methyltrimethoxysilane, dimethyldimethoxysilane, phenyltrimethoxysilane, vinyltrimethoxysilane, tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane and tetrabutoxysilane. After hydrolysis or partial hydrolysis of these compounds, the silicon atoms therein may be bonded to C, OH or OR groups, but a substantial portion of the material is believed to be condensed in the form of soluble Si-O-Si resins. The precursor most preferably comprises compounds in which each R is independently an diphatic substituent of 1-4 carbon atoms, and n is 0 or 1. Compounds in which n = 2 or 3 are generally not used alone as volatile cyclic structures are generated during pyrolysis, but small amounts of said compounds may be cohydrolyzed with other silanes to prepare useful preceramic materials.
  • The above silica precursor coating material may also contain other ceramic oxide precursors. Examples of such ceramic oxide precursors include compounds of various metals such as aluminum, titanium, zirconium, tantalum, niobium and/or vanadium as well as various non-metallic compounds such as those of boron or phosphorous which may be dissolved in solution, hydrolyzed and subsequently pyrolyzed, at relatively low temperatures and relatively rapid reaction rates to form ceramic oxide coatings.
  • The above ceramic oxide precursor compounds generally have one or more hydrolyzable groups bonded to the above metal or non-metal, depending on the valence of the metal. The number of hydrolyzable groups to be included in these compounds is not critical as long as the compound is soluble in the solvent. Likewise, selection of the exact hydrolyzable substituent is not critical since the substituents are either hydrolyzed or pyrolyzed out of the system. Typical hydrolyzable groups include alkoxy, such as methoxy, propoxy, butoxy and hexoxy, acyloxy, such as acetoxy or other organic groups bonded to said metal or nonmetal through an oxygen such as acetylacetonate. Specific compounds, therefore, include zirconium tetracetylacetonate, titanium dibutoxy diacetylacetonate, aluminum triacetylacetonate and tetraisobutoxy titanium.
  • When the silica precursor is to be combined with one of the above ceramic oxide precursors, generally it is used in an amount such that the final ceramic coating contains 70 to 99.9 percent by weight SiO2.
  • According to the process of the invention, the above silica precursor and, optionally, any ceramic oxide precursors are applied to the surface of a substrate. This can be accomplished in any manner, but a preferred method involves dissolving the silica precursor in a solvent to form a solution or dispersion which is applied to the surface of the substrate. Various facilitating measures such as stirring and/or heating may be used to dissolve or disperse the silica precursor and create a more uniform application solution. Solvents which may be used include any agent or mixture of agents which will dissolve or disperse the silica precursor to form a homogenous solution without affecting the resultant coating. These solvents can include, for example, alcohols such as ethyl or isopropyl, aromatic hydrocarbons such as benzene or toluene, alkanes such as n-heptane or dodecane, ketones, esters, glycol ethers or cyclic dimethylpolysiloxanes, in an amount sufficient to dissolve the above materials to low solids. Generally, enough of the above solvent is used to form a 0.1-50 weight percent solution.
  • If a solution method is used, the solution comprising the silica precursor, solvent and, optionally, a modifying ceramic oxide precursor is then coated onto the substrate. The method of coating can be spin coating, dip coating, spray coating or flow coating. Other equivalent means, however, are also deemed to be within the scope of this invention.
  • The solvent is then allowed to evaporate from the coated substrate resulting in the deposition of a silica precursor coating. Any suitable means of evaporation may be used such as simple air drying by exposure to an ambient environment, by the application of a vacuum or mild heat (eg., less than 50°C) or during the early stages of the heat treatment. It is to be noted that when spin coating is used, the additional drying period is minimized as the spinning process drives off the solvent.
  • Once the silica precursor coating is applied, it is then heated in an environment containing nitrous oxide at a temperature sufficient to convert it to a silica-containing material. During this conversion, factors such as nitrous oxide gas concentration, gas exposure time, temperature and heating time all need to be controlled.
  • The nitrous oxide used in this process is known in the art and commercially available. It may be used in this invention in its neat form or it may be diluted in additional gases (eg., inert gases such as argon or nitrogen or reactive gases such as air, ammonia or amines) to a concentration sufficient to convert the silica precursor to silica at a desirable rate under the temperature conditions chosen.
  • The silica precursor coating is generally exposed to this gas for a time sufficient to convert the silica precursor to silica. Generally, times in the range of several minutes to several hours are useful (eg., 2 minutes to 2 hours). This exposure can occur during the ramp-up, during the heat soak or during ramp-down.
  • As noted above, it is also contemplated herein that the silica precursor may be concomitantly or sequentially exposed to other reactive gases which assist in conversion. For instance, it is within the scope of this invention to also expose the silica precursor to moisture (eg., steam), ammonia, amines or other oxidizing gases.
  • Generally, the temperatures useful herein are in the range of 100°C. to 600°C. Higher and lower temperatures, however, are also contemplated in the invention. For example, lower temperatures may be used but they often result in incomplete conversion of the silica precursor and insufficient densification of the ceramic. Similarly, higher temperatures (eg., 1000°C.) may be used but the need for nitrous oxide is diminished since the silica precursors can generally be converted to silica at such temperatures in air.
  • Generally, the coated substrates are heated under the nitrous oxide containing environment for a time sufficient to convert the silica precursor to silica. Time periods in the range of a few minutes for very thin films to several hours for very thick films, depending on the temperature, are generally useful herein. It is particularly preferred to heat the coated substrates at a temperature of 200-500°C. for 1-3 hours.
  • Any method of heating such as the use of a quartz tube furnace, a convection oven, reverse direction processing as described in US Patent Application 07/633,707, now allowed, and assigned to the same assignee hereof or radiant or microwave energy is generally functional herein. Similarly, the rate of heating is generally not a critical factor, but it is most practical and preferred to heat the substrate as rapidly as possible.
  • By the above methods a thin (less than 2 micrometers) silica-containing ceramic planarizing coating is produced on the substrate. The coating smooths the irregular surfaces of various substrates and has excellent adhesive properties. In addition, the coating may be covered by other coatings such as additional SiO2 layers, silicon containing coatings, silicon carbon containing coatings, silicon nitrogen containing coatings, silicon oxygen nitrogen containing coatings and/or silicon nitrogen carbon containing coatings. Such multiple layer coatings are known in the art and many are described in U.S. Patent No. 4,756,977.
  • Coatings produced by the instant invention possess low defect density and are useful on electronic devices as protective coatings, as corrosion resistant and abrasion resistant coatings, as temperature and moisture resistant coatings, as dielectric layers and as a diffusion barrier against ionic impurities such as sodium and chloride.
  • The following examples are provided so that one skilled in the art may more readily understand the invention.
    • Example 1
  • A 2.5 cm (1 inch) square silicon wafer was spin coated with a 10 wt. % solution of partially hydrolyzed ethylorthosilicate in isopropyl alcohol and n-Butanol solvents at a spin speed of 3000 RPM for 20 seconds. The coated wafer was heated to 350°C. for 3 hours in an environment comprising 100% nitrous oxide. FTIR analysis after the heat treatment showed only a trace of SiOH remained. The coating thickness was 289 nm (2888 angstroms) and the refractive index was 1.452 at 405 nm.
    • Example 2
  • A 2.5 cm (1 inch) square silicon wafer was spin coated with a 10 wt. % solution of partially hydrolyzed ethylorthosilicate in isopropyl alcohol and n-butanol solvents at a spin speed of 3000 RPM for 20 seconds. The coated wafer was heated to 425°C. for 3 hours in an environment comprising 100% nitrous oxide. FTIR analysis after the heat treatment showed essentially all of the SiOH was removed. The coating thickness was 286 nm (2863 angstroms) and the refractive index was 1.456 at 405 nm.

Claims (9)

  1. A method of forming a silica-containing ceramic coating on a substrate comprising:
    applying a silica precursor containing coating comprising hydrolyzed or partially hydrolyzed RnSi(OR)4-n on the substrate, in which each R is independently an aliphatic, alicyclic or aromatic substituent of 1-20 carbon atoms and n is 0-3; and
    heating the coated substrate in an atmosphere comprising nitrous oxide at a temperature between 100 and 600°C. for 1 to 3 hours to convert the silica precursor containing coating to a silica-containing ceramic coating.
  2. The method of claim 1 wherein the silica precursor containing coating is applied to the substrate by a process which comprises coating the substrate with a solution comprising a solvent and the silica precursor and then evaporating the solvent.
  3. The method of claim 2 wherein said solution is coated onto the substrate by spray coating, dip coating, flow coating or spin coating.
  4. The method of claim 1 wherein the silica precursor material comprises hydrolyzed or partially hydrolyzed compounds of the formula RnSi(OR)4-n, in which each R is independently an aliphatic substituent of 1-4 carbon atoms and n is 0-1
  5. The method of claim 1 wherein the silica precursor containing coating also contains modifying ceramic oxide precursors comprising a compound containing an element selected from titanium, zirconium, aluminum, tantalum, vanadium, niobium, boron and phosphorous wherein the compound contains at least one hydrolyzable substituent selected from alkoxy or acyloxy and the compound is present in an amount such that the silica coating contains 0.1 to 30 percent by weight of modifying ceramic oxide.
  6. The method of claim 1 wherein the heating atmosphere also contains an inert gas.
  7. The method of claim 1 wherein the heating atmosphere also contains an additional reactive gas.
  8. The method of claim 1 wherein the heating atmosphere also contains moisture.
  9. The method of claim 1 wherein the coated substrate is only exposed to the nitrous oxide during a portion of the heating.
EP93308383A 1992-11-02 1993-10-21 Curing silica precursors by exposure to nitrous oxide Expired - Lifetime EP0605090B1 (en)

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JPH06206784A (en) 1994-07-26
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US5820923A (en) 1998-10-13
JP3362073B2 (en) 2003-01-07
DE69311690D1 (en) 1997-07-24

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